Pathophysiological role of platelets and platelet system in acute pancreatitis

Microvasc Res. 2008 Aug;76(2):114-23. doi: 10.1016/j.mvr.2008.05.001. Epub 2008 Jun 10.

Abstract

The most successful approach for restoring normal long-term glucose homeostasis in type I diabetes mellitus is whole-organ pancreas transplantation. Graft pancreatitis is observed in up to 20% of patients and may lead to loss of the transplanted organ. Several pathophysiological events have been implicated in this form of pancreatitis. The most important cause of early graft pancreatitis is ischemia/reperfusion (I/R)-related disturbance of microvascular perfusion with subsequent hypoxic tissue damage. Recently, considerable evidence accumulated that, among a variety of other pathophysiological events, the activation of platelets can contribute to I/R injury in the course of acute pancreatitis experimentally and clinically. This review summarizes the events affecting platelet function and, therefore, pancreatic microcirculation leading to acute pancreatitis. Therapeutic approaches and own results are presented.

Publication types

  • Review

MeSH terms

  • Animals
  • Blood Platelets / physiology*
  • Humans
  • Microcirculation / metabolism
  • Microcirculation / physiopathology
  • Pancreas / blood supply
  • Pancreas / pathology
  • Pancreas / physiopathology
  • Pancreas Transplantation / adverse effects
  • Pancreatitis, Acute Necrotizing / etiology
  • Pancreatitis, Acute Necrotizing / physiopathology*
  • Pancreatitis, Acute Necrotizing / therapy
  • Postoperative Complications / etiology
  • Postoperative Complications / physiopathology*
  • Postoperative Complications / therapy
  • Reperfusion Injury / etiology
  • Reperfusion Injury / physiopathology